Variant report

Variant	rs11765325
Chromosome Location	chr7:104206662-104206663
allele	A/G
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

Extended variants
information (count: 12 )
Associated
traits (count: 0)

rSNPs within LD-proxies of this variant (count:12)

rs_ID	r²[population]
rs10270298	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11766963	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11770655	0.87[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs11772285	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17138713	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs17138748	0.92[AFR][1000 genomes];1.00[AMR][1000 genomes];0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73409771	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73409775	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73409785	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73409787	0.97[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73409791	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs73409795	0.97[AFR][1000 genomes];1.00[AMR][1000 genomes];1.00[EUR][1000 genomes];1.00[ASN][1000 genomes]

No data

Chromatin state (count:1 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr7:104206600-104214000	Weak transcription	Brain Germinal Matrix	brain

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Input of quick search could be:

dbSNP/dbVar ID: rs12345 /nsv7879
a single nucleotide as 0-based coordinates: chr1:12345
chromosomal regions: chr1:12345-34567

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